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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601757Generated: October 29, 2026

Pyridine → 3-Benzothiazol-2-yl-3,5-dichloro-1,3-dihydroindol-2-one

https://huagongshe.com/reaction/601757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantThionyl ChlorideHCID 24386—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-Benzothiazol-2-yl-5-chloro-3-hydroxy-1,3-dihydroindol-2-oneHCID 57517750—
SolventDichloromethaneHCID 6344—
Product3-Benzothiazol-2-yl-3,5-dichloro-1,3-dihydroindol-2-oneHCID 57517751—

Reaction Conditions

Temperature0 °C

Reaction Steps

Pyridine (0.57 ml) and thionyl chloride (0.42 ml) were successively added to an ice-cooled solution of the intermediate from step A (1.27 g, 4.0 mmol) in dichloromethane (40 ml). The reaction mixture was stirred at 0° C. for 1 h and then saturated ammonium chloride solution was added. The organic phase was dried over magnesium sulfate, filtered and concentrated under reduced pressure. The crude intermediate was rapidly employed without further purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902379B2
Source datasetuspto-grants-2011_03
ORD IDord-d32d109e19234893bb42c27cd7b101a9
Source noteuspto-grants-2011_03